California chipmunks, (Best and Granai, 1994), can be found throughout the San Bernardino and San Jacinto mountains of southern California in a series of disjunct populations. Their range also extends southward, across desert ranges into Baja California, reaching as far south as the Sierra de San Francisco.
They are typically found at elevations between 760 and 600 m (Callahan, 1977). These chipmunks occupy lower Sonoran, upper Sonoran, transition, and Canadian life zones (Best and Granai, 1994). Their habitat can also be described by the botanical wildlife in the areas; usually these are pinyon-juniper or pine-oak forests, often with manzanita or sage, and nearby rocky outcroppings (Best and Granai, 1994). North of San Gorgonio Pass, Tamias merriami at elevations above pinyon-juniper habitat. However, the opposite occurs in communities south of San Gorgonio Pass. occurs alone in the Santa Rosa Mountains (Callahan, 1977). (Best and Granai, 1994; Callahan, 1977)is replaced by
Through much of their range, California chipmunks are indistinctly colored. During the warmer summer months, the head is pale gray shaded with cinnamon, bordered on the sides with snuff brown, extending down to the snout as clay-redbrown. The facial stripes are dark brown, with blackish stripes around the eyes, offset by paler-gray stripes. On the dorsal side of the trunk, pelage has dark russet-brown stripes offset by a median pair of the pale gray stripes. The ventral pelage is creamy white. During the winter the pelage is very similar, but the dorsal stripes are more pronounced and the sides of the chipmunk become a pale brown (Best and Granai, 1994).
Average total length of these animals is 208 to 240 mm, of which the tail comprizes 91 to 99 mm. The hindfoot varies between 33 and 35 mm, and the weight varies betweeen 56 and 90 g (Callahan, 1977). Females are typically larger than males in cranium length, rostral length, zygomatic breadth, and several characters, but males have wider nasals than females (Best and Granai, 1994).
Tamias merriami, which has an overlapping range with California chipmunks, is superficially similar to . However, may be readily distinguished by the shape of the ossa genitalia, a longer hind foot, and a more rounded cranium. In the summer, also has paler adult pelage with less yellow with more reddish dorsal stripes than T. merriami (Callahan, 1977).
The breeding season ofis long, starting in January and extending into July (Best and Granai, 1994). During this season, a female can have more than two litters of 3 or 4 young each (Best and Granai, 1994). The gestation period for these chipmunks is approximately one month. The mothers often do not molt their winter pelage until after the young are independent (Callahan, 1976). Young are typically independent by the age of 8 weeks (Best and Granai, 1994).
Although there are no data for this species, in other members of the genus Tamias, the young reach independence during the season of birth, and are capable of breeding in the following breeding season. It is likely that is similar to other members of the genus in this regard. (Best and Granai, 1994; Callahan, 1976)
There is little information published regarding longevity in this species, but oneis known to have lived in captivity for 10 years (Best and Granai, 1994).
This diurnal chipmunk is active throughout the year. The greatest amount of foraging and activity takes place in early morning and late afternoon. (Callahan, 1977). (Blankenship and Brand, 1987; Callahan, 1977)often creates burrows in logs or steep hillsides that are protected by the use of large boulders (Best and Granai, 1994).
uses vocalizations such as the chuck, trill, chatter, and chip (Blankenship and Brand, 1987). Calls are thought to be somewhat species specific, and may be a way for to recognize potential mates. Species specific vocalizations might play a role in reproductive isolation of sympatric species. (Blankenship adn Brand, 1987).
Although not specifically reported for this species, it is likely that California chipmunks use visual cues such as body positioning, tail position, and tail flicking in their communication, as these behaviors are common in most species in the genus. It can also be assumed that tactile communication occurs, especially during mating and between mothers and their offspring. (Blankenship and Brand, 1987)
Reports of predation on these small mammals are not available. However, California chipmunks can use nearby rocks, logs, brush, and trees for cover and to hide from predators. Predation is likely to come from carnivorous animals such as hawks, foxes, and coyotes (Best and Granai, 1994).
These chipmunks probably play some role in seed dispersal, as they transport seeds from the places they are found to feeding stations and food caches. They are likey to be important in local food webs, also, although the extent to which various predatory animals may depend upon them is not known. (Blankenship, 1999)
These chipmunks have no known impact on humans.
These chipmunks have no known negative impact on humans.
These animals have a very limited distribution. As such, it is especially important to protect their habitat to ensure that the species will survive into the future.
Faith Chinnock (author), California State Polytechnic University, Pomona, Rebecca Cole (author), California State Polytechnic University, Pomona, John Demboski (editor, instructor), California State Polytechnic University, Pomona.
Nancy Shefferly (editor), Animal Diversity Web.
living in the Nearctic biogeographic province, the northern part of the New World. This includes Greenland, the Canadian Arctic islands, and all of the North American as far south as the highlands of central Mexico.
uses sound to communicate
young are born in a relatively underdeveloped state; they are unable to feed or care for themselves or locomote independently for a period of time after birth/hatching. In birds, naked and helpless after hatching.
having body symmetry such that the animal can be divided in one plane into two mirror-image halves. Animals with bilateral symmetry have dorsal and ventral sides, as well as anterior and posterior ends. Synapomorphy of the Bilateria.
uses smells or other chemicals to communicate
having markings, coloration, shapes, or other features that cause an animal to be camouflaged in its natural environment; being difficult to see or otherwise detect.
animals that use metabolically generated heat to regulate body temperature independently of ambient temperature. Endothermy is a synapomorphy of the Mammalia, although it may have arisen in a (now extinct) synapsid ancestor; the fossil record does not distinguish these possibilities. Convergent in birds.
forest biomes are dominated by trees, otherwise forest biomes can vary widely in amount of precipitation and seasonality.
an animal that mainly eats fruit
an animal that mainly eats seeds
An animal that eats mainly plants or parts of plants.
offspring are produced in more than one group (litters, clutches, etc.) and across multiple seasons (or other periods hospitable to reproduction). Iteroparous animals must, by definition, survive over multiple seasons (or periodic condition changes).
having the capacity to move from one place to another.
This terrestrial biome includes summits of high mountains, either without vegetation or covered by low, tundra-like vegetation.
the area in which the animal is naturally found, the region in which it is endemic.
scrub forests develop in areas that experience dry seasons.
breeding is confined to a particular season
remains in the same area
reproduction that includes combining the genetic contribution of two individuals, a male and a female
places a food item in a special place to be eaten later. Also called "hoarding"
uses touch to communicate
that region of the Earth between 23.5 degrees North and 60 degrees North (between the Tropic of Cancer and the Arctic Circle) and between 23.5 degrees South and 60 degrees South (between the Tropic of Capricorn and the Antarctic Circle).
Living on the ground.
uses sight to communicate
reproduction in which fertilization and development take place within the female body and the developing embryo derives nourishment from the female.
Best, T., N. Granai. 1994. Mammalian Species, 472: 1-6..
Blankenship, D. 1999. California chipmunk| Tamias obscurus . Pp. 369-370 in D Wilson, S Ruff, eds. The Smithsonian Book of North American Mammals. Washington and London: The Smithsonian Institution Press in Association with the American Society of Mammalogists.
Blankenship, D., L. Brand. 1987. Geographic Variation in Vocalizations of Tamias obscurus and T. merriami . Bulletin of Southern California Academy of Sciences, 86: 126-135.
Callahan, J. 1977. Diagnosis of Eutamias obscurus (Rodentia: Sciuridae). Journal of Mammalogy, 58: 188-201.
Callahan, J. 1976. Systematics and Biogeography of Eutamias obscurus . University of Arizona: Department of General Biology.